A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578258



Internal ID16018981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137713..1152657hg38UCSC Ensembl
Innerchr19:1137712..1152656hg19UCSC Ensembl
Innerchr19:1088712..1103656hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3814945
hg1914945
hg1814945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6187n54
Supporting Variantsnssv891755, nssv891756
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578258
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer